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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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10 records meeting your search criteria returned- Product Code: FCG Product Problem: Defective Device Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE 01/14/2022
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE 11/30/2021
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U401SX 11/09/2021
OLYMPUS MEDICAL SYSTEMS CORP. BIOPSY NEEDLE 09/24/2021
OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE ASPIRATION NEEDLE NA-U401SX 08/04/2021
UNITED STATES ENDOSCOPY GROUP, INC CARR-LOCKE INJECTION NEEDLE 09/18/2019
CAREFUSION / BECTON DICKINSON AND COMPAN CAREFUSION COAXIAL TEMNO EVOLUTION 09/17/2018
MERIT MEDICAL SYSTEMS INC. COAXIAL BIOPSY NEEDLE 09/11/2018
OLYMPUS MEDICAL SYSTEMS CORP. EBUS 08/15/2018
CAREFUSION, INC JAMSHIDI BONE MARROW NEEDLES 03/02/2017
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